A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259335



Internal ID20468553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114394183..114394183hg38UCSC Ensembl
chr11:114264905..114264905hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751045
Supporting Variants
Samples
Known GenesC11orf71
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259335
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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